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Pantoprazole Sodium

NDC 68071-1963, Pantoprazole Sodium, tablet, delayed release, from NuCare Pharmaceuticals, Inc..

Product NDC
68071-1963
Status
Listed
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090074
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-1963 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PANTOPRAZOLE SODIUM40 mg/1

Pharmacologic classes

Proton Pump Inhibitor [EPC]; Proton Pump Inhibitors [MoA]

Package NDCNDC-11Package
68071-1963-36807119630330 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-1963-3)
68071-1963-46807119630414 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-1963-4)
68071-1963-66807119630660 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-1963-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4fbec80c-b38d-122c-e054-00144ff88e88

Use it

Look up 68071-1963 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-1963 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-1963. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.